2-acylimino-1,3-diazacycloalkanes

ABSTRACT

1-R1-2-TRIMETHOXYBENZOYLIMINO-1,3-DIAZACYCLOALKANES, E.G. THOSE OF THE FORMULA   (3,4,5-TRI(CH3-O-)PHENYL)-CO-N=C&lt;(-N(-R1)-(CH2)N-N(-R3)-)   R1=ALIPHATIC OR CYCLOALIPHATIC RADICAL R3=H, ALKYL OR ALKANOYL N=2-4 OR SALTS THEREOF EXHIBIT HYPNOTIC EFFECTS.

United States Patent 3,758,473 2-ACYLIMINO-I,3-I)IAZACYCLOALKANES Robert Armistead Lucas, Mendham, and Herbert Morton Blatter, Summit, N.J., assignors to Ciba-Geigy Corporation, Ardsley, N.Y.

No Drawing. Continuation-impart of application Ser. No.

129,185, Mar. 29, 1971, which is a continuation-inpart of application Ser. No. 26,433, Apr. 7, 1970, which is a continuation-impart of application Ser. No. 884,322, Dec. 11, 1969, now Patent No. 3,627,889, which in turn is a continuation-in-part of application Ser. No. 839,704, July 7, 1969, now Patent No. 3,655,895. This application June 29, 1971, Ser. No. 158,115

Int. Cl. C07d 49/30, 51/18, 53/07 US. Cl. 260--256.4 H Claims ABSTRACT OF THE DISCLOSURE 1 R -2-trimethoxybenzoylimino-1,3-diazacycloalkanes, e.g. those of the formula R =aliphatic or cycloaliphatic radical R =H, alkyl or alkanoyl n=24 or salts thereof exhibit hypnotic effects.

CROSS-REFERENCES TO RELATED APPLICATIONS This is a continuation-in-part of application Ser. No. 129,185, filed Mar. 29, 1971, which in turn is a continuation-in-part of application Ser. No. 26,433, filed Apr. 7, 1970, which in turn is a continuation-in-part of application Ser. No. 884,322, filed Dec. 11, 1969, (now Pat. No. 3,627,889) which in turn is a continuation-in-part of application Ser. No. 839,704, filed July 7, 1969 (now Pat. No. 3,655,895).

BACKGROUND OF THE INVENTION SUMMARY OF THE INVENTION The present invention concerns and has for its object the provision of new 5 to 7 ring-membered 1-R -2-trimethoxybenzoylimino-1,3-diazacycloalkanes (or of the tautomeric 1 R -Z-trimethoxybenzoylamino-1,3-diazacycloalkanes or of the isomeric 1-R -2imino-3-trimethoxybenzoyl-1,3-diazacycloalkanes) or of N-alkyl or acyl derivatives or salts thereof, wherein R is an unsubstituted or substituted aliphatic or cycloaliphatic radical, preferably of those corresponding to Formula I 3,758,473 Patented Sept. 11, 1973 ice in which R, is lower alkyl, alkenyl or alkynyl, (hydroxy, lower alkoxy or di-lower alkylamino)-lower alkyl wherein the oxygen or nitrogen atom is separated from the ring-nitrogen atom by at least 2 carbon atoms, 3 to 7 ring-membered cycloalkyl, cycloalkenyl, cycloalkyl-lower alkyl or cycloalkenyl-lower alkyl, R is trimethoxybenzoyl, R is hydrogen, lower alkyl, alkanoyl or aralkanoyl and alk is lower alkylene separating the adjacent nitrogen atoms by 2 to 4 carbon atoms, or of salts thereof, as well as of corresponding pharmaceutical compositions and of methods for the preparation and application of these products. Said compositions are useful sedative-hypnotic agents.

DESCRIPTION OF THE PREFERRED EMBODIMENTS The substituent R represents preferably lower alkyl, lower alkenyl, lower alkynyl or said (hydroxy, lower alkoxy or di-lower alkylamino)-lower alkyl radicals, e.g. methyl, ethyl, nor i-propyl or -butyl, 3-methylbutyl, lor Z-pentyl, -hexyl or -heptyl allyl, methallyl, Z-butenyl, 2-but-2-enyl, 2- or 3-pentenyl, 2-pent-2-enyl or 2-hexenyl; propargyl, 2-butynyl or 2-hex-3-ynyl; 2-(hydroxy, methoxy, ethoxy, dimethylamino, diethylamino, di-n or i-propylamino)-ethyl or -propyl, 3-(hydroxy, methoxy or dimethylamino)-propyl or -butyl; but also 3 to 7 ringmembered cycloalkyl, cycloalkenyl, cycloalkyl-lower alkyl or cycloalkenyl-lower alkyl radicals, e.g. cyclopropyl, cyclopentyl or cyclohexyl; lor 2-cyclopentenyl, -cyclohexenyl or -cycloheptenyl; cyclopropylmethyl, cyclopentylmethyl, 2-cyclopentylethyl or cyclohexylmethyl, l-cyclopentenylmethyl, 2-cyclopent-l-enylethyl or l-cyclohexenylmethyl. The term lower referred to above and hereinafter in connection with organic radicals or compounds respectively, defines such with up to 7, preferably up to 4, carbon atoms.

The trimethoxybenzoyl radical R contains the methoxy groups in any of the 5 positions of the phenyl nucleus thereof. It preferably represents 3,4,5-trimethoxybenzoyl, but also, for example, 2,3,4- or 2,4,5-trimethoxybenzoyl.

Acyl derivatives of the invention are derived from aliphatic or aromatic carboxylic acids, preferably of lower alkanoic or aralkanoic acids. Thus the radical R represents, for example, acetyl, propionyl or privalyl; benzoyl, mono-, dior trimethoxybenzoyl or phenylacetyl.

The alkylene moiety alk, separating the nitrogen atoms of the 1,3-diazacycloalkane moiety by 2-4 carbon atoms, preferably represents 1,2-ethylene or 1,3-propylene but also, for example, 1,2-propylene, 1,2-, 1,3-, 1,4-, or 2,3-butylene, 1,2-, 1,3-, 1,4-, 2,3- or 2,4-pentylene, -hexylene or -heptylene.

The compounds of the invention exhibit valuable pharmacological properties. Besides central nervous system depressing eifects, such as sedative and skeletal muscle relaxing effects, they predominantly exhibit hypnotic effects. This can be demonstrated in animal tests, using advantageously mammals, such as mice, rats, rabbits, cats, dogs or monkeys as test objects. The compounds of the invention can be applied to the animals enterally or parenterally, e.g. orally, intraperitoneally or intravenously, for example, in gelatin capsules or in the form of aqueous solutions or suspensions. The oral dosage may range in the lower animals, e.g. mice or rats, between about 1 and about 500 mg./kg./day, preferably between about 5 and about 200 mg./kg./day, and in the higher animals, e.g. dogs or monkeys, advantageously between about 10 and about 50 mg./kg./day. The effect on the spontaneous and induced motor activity is observed in the mice jiggle cage, light box or rotorod test systems, wherein a. depression is recorded after oral medication. Oral doses in the cat induce a sleep-like state (constricted pupils and relaxed nictitating membranes) from which the animal can be aroused without showing motor incoordination. Oral doses produce also sleep in dogs and monkeys, wherein the animals assume a normal position. Low nitravenous doses produce in the cat depression of several reflexes, e.g. the flexor and patellar reflex, and in the rabbit a lesser reduction of the respiratory rate as with conventional hypnotics at equi-hypnotic doses. Accordingly, the compounds of the invention are useful sedative-hypnotic agents, for example, in the treatment or management of restlessness and emotional tension, for suppression of anxiety and neurotic manifestations, and preferably for the induction of sleep. They are also useful intermediates in the preparation of other valuable products, especially of pharmacologically active compounds.

Particularly useful are the compounds of Formula I, in which R is alkyl with up to 4 carbon atoms, R is 3,4,5- trimethoxybenzoyl, R is hydrogen or alkyl with up to 4 carbon atoms and alk is 1,2-ethylene, 1,2- or 1,3-propylene, as well as those compounds of Formula I, in which R is also alkenyl or alkynyl with up to 4 carbon atoms, R is also alkanoyl with up to 4 carbon atoms and alk is also 1,2-, 1,3-, 1,4- or 2,3-butylene, as well as those compounds of Formula I, in which R is also (hydroxy, alkoxy or dialkylamino)-alkyl wherein alkyl contains up to 4 carbon atoms and the oxygen or nitrogen atom therein is separated from the ring-nitrogen atom by at least 2 carbon atoms and R is also 2,3,4- or 2,4,5-trimethoxybenzoyl, or therapeutically acceptable acid addition salts of all these compounds.

Especially valuable are compounds of Formula II in which R is methyl, ethyl, n-propyl, allyl or Z-dimethylaminoethyl, R is hydrogen, methyl or acetyl and n is an integer from 2 to 4, preferably 3, more particularly the 1- methyl 2 (3,4,S-trimethoxybenzoylimino)-hexahydropyrimidine, or therapeutically acceptable acid addition salts thereof, which exhibit a high order of sedative-hypnotic activity and low toxicity, preferably afteroral application.

The compounds of this invention are prepared according to methods known per se. For example, the process for their preparation consists in:

(a) acylating a 1 R -2-imino-3-R -1,3-diazacycloalkane with a trimethoxybenzoic acid or a reactive functional derivative thereof or (b) converting in an N-Y-trimethoxybenzamide or -imide, in which Y is a substituent conversible into a 1-R -3-R -1,3-diazacyclo 2 (alkenyl or alkylidene) radical respectively, Y into said radical or (c) methylating a l R -3-R -2-trihydroxybenzoylimino- 1,3-diazacycloalkane or (d) hydrogenating a l-R -2-R -imino-3-R -1,3-diazacycloalkene or -alkadiene and, if desired, converting any resulting 5 to 7 ring-membered compound into another compound of the invention.

The acylation according to item (a) is advantageously performed with a reactive functional derivative of the trimethoxybenzoic acid, such as a lower alkyl ester, halide, e.g. chloride or bromide, or anhydride thereof, e.g. the simple or a mixed anhydride with any other suitable acid, such as a lower alkyl carbonic acid.

In the starting material mentioned under item (b), the substituent Y is, for example, a l-unsubstituted 3-R l,3- diazacyclo-Z-(alkenyl or alkylidene) radical, which can be substituted in the 1-position, for example, by reaction with a reactive ester of the alcohol R OH, for example, that of a strong mineral or sulfonic acid, such as a hydrohalic acid, e.g. hydrochloric, hydrobromic or hydroiodic acid, sulfuric acid or a lower alkane or benzene sulfonic acid, e.g. methane-, ethaneor p-toluenesulfonic acid. Another substituent Y is, for example, a cyano or dialkylmercaptomethylene group, e.g. dimethylmercaptomethylene, or a thiocarbamoyl or S-alkyl-isothiocarbamoyl group or the NR or N'-R derivatives thereof. The corresponding starting material, ie an N-R -cyanamide, a dialkyl NR -dithiocarbaminate, NR -thiourea, N,N'-bis-R thiourea or advantageously an S-alkylNR -isothiourea or S-alkylN,N'bis-R -isothiourea respectively, is condensed with the diamine R NHalkNH-'-R wherein R is hydrogen or lower alkyl, in order to obtain the compounds of the invention.

The methylation according to item (c) is advantageously performed with a diazomethane, but also with a reactive ester of methanol, e.g. such mentioned above for R OH.

The hydrogenation according to item (d) is preferably carried out with catalytically activated or nascent hydro gen, for example hydrogen applied in the presence of nickel, platinum or palladium catalysts or generated electrolytically or by the action of metals on acids or alcohols, such as heavy metals, e.g. zinc or iron, on mineral or carboxylic acids, or light metals, e.g. sodium or magnesium, on alkanols.

The compounds of the invention so obtained, can be converted into each other according to methods known per se. For example, resulting compounds of Formula I in which R is hydrogen, can be acylated or alkylated in 3-position as shown under items (a) and (b), i.e. with reactive functional derivatives of aliphatic or aromatic acids or reactive esters of lower alkanols respectively. Resulting compounds in which R is an acyl group, e.g. trimethoxybenzoyl or lower alkanoyl, can be hydrolyzed, e.g. by the careful application of acidic or alkanoline hydrolyzing agents, such as aqueous mineral acids or alkalis, e.g. hydrohalic or sulfuric acids, or alkali metal, e.g. sodium or potassium, hydroxides, carbonates or bicarbonates.

The compounds of the invention are obtained in the free form or in the form of their salts, depending on the conditions under which the above process is carried out. A resulting free base can be converted into a corresponding acid addition salt, for example by reacting it with an inorganic or organic acid, preferably a therapeutically useful acid, or with a corresponding anion exchange preparation, and isolating the desired salt. An acid addition salt may be converted into the free compound by treatment with a base, e.g. a metal hydroxide, ammonia or a hydroxyl ion exchange preparation. Therapeutically useful acids are, for example, inorganic acids, such as strong metalloidic acids, for example, hydrohalic, e.g. hydrochloric, hydrobromic, sulfuric, phosphoric, nitric or perchloric acid, or organic acids, such as carboxylic or sulfonic acids, e.g. formic, acetic, propionic, succinic, glycolic, lactic, malic, tartaric, citric, ascorbic, maleic, hydroxymaleic, pyroracemic, phenylacetic, benzoic, 4-aminobenzoic, anthranilic, 4-hydroxybenzoic, salicylic, amino-salicylic, embonic, nicotinic, methanesulfonic, ethanesulfonic, hydroxyethanesulfonic, ethylenesulfonic, halogenbenzenesulfonic, toluenesulfonic, naphthalenesulfonic, sulfanilic and cyclohexylsulfamic acid; methionine, tryptophan, lysine and arginine.

These or other salts, for example, the picrates, can also be used for purification of the resulting free compounds, which are converted into salts, the salts separated and the free compounds liberated from the salts. In view of the close relationship between the free compounds and the compounds in the form of their salts, Whenever a compound is referred to in this context, a corresponding salt is also intended, provided such as possible or appropriate under the circumstances.

Resulting mixtures of isomers can be separated into the single isomers by methods in themselves known, e.g. by fnactional distillation, crystallization and/or chromatography. Racemic products can likewise be resolved into the optical antipodes, for example, by separation of diastereomeric salts thereof, e.g. by the fractional crystallization of dor l-tartrates.

The above reactions are carried out according to standard methods, in the presence or absence of diluents, preferably such as are inert to the reagents and are solvents thereof, of catalysts, condensing, neutralizing agents and/ or inert atmospheres, at low temperatures, room temperature or elevated temperatures, at atmospheric or superatmospheric pressure. For example, in the above acylation or alkylation reactions, the generated mineral or sulfonic acid may be neutralized with inorganic or Organic bases, such as alkali or alkaline earth metal carbonates or bicarbonates, tri-lower alkylamines or pyridine.

The invention also comprises any modification of the above process, wherein a compound resulting as an intermediate at any stage thereof, is used as starting material and the remaining steps are carried out or the process is discontinued at any stage thereof, or in which the starting material is formed under the reaction conditions or is used in the form of its salts or reactive derivatives. For example, in the reaction according to item (b) with compounds in which Y is dialkylmercaptomethylene, the intermedite formed first is an SalkylN-R -isothiourea, which ring-closes in a second step under the influence of heat and/or acidic catalysts. Also in the methylation reaction according to item (c), dihydroxymethoxyand dimethoxy-hydroxybenxoylimino intermediates are formed during the etherification procedure which, of course, can also be chosen as starting materials. The hydrogenation according to item (d) may also be carried out stepwise, for example, a 1-R -2-R -imino-1,3-diazacycloalkadiene can first be reduced with sodium borohydride to the corresponding 1-R -2-R -imino 3H 1,3-diazacycloalkene, which latter or its 3-R -derivative, is subjected to hydrogenation, Preferred are starting materials, which lead to those compounds of the invention, which are indicated above as the preferred embodiments of the invention.

The starting materials used are known or, if new, may be prepared according to the methods illustrated in the examples herein. For example, the starting material mentioned under item (a) is prepared in accordance with the methods described in US. Pat. No. 3,027,370 or British Pat. No. 765,547. The starting material mentioned under item (b) in which Y is a l-unsubstituted 3-R -1,3- diazacyclo-Z-(alkenyl or alkylidene) radical, can be obtained either by the acylation method according to item (a) or from corresponding 1-benzyl-2-R -3-R -l,3-diazacycloalkanes, which are subjected to reductive cleavage, e.g. with the use of catalytically activated hydrogen. The starting material, in which Y is advantageously bis-(lower alkylmercapto)-methylene, can be obtained by addition of lower alkylmercaptanes to trimethoxybenzoylisothiocyanates and reacting the resulting dithiourethanes with a lower alkyl halide or sulfonate. The thioureas or isothioureas also mentioned under item (b) as well as the starting material mentioned under items (c) and (d) can be prepared analogous to the acylation process described under item (a), i.e. by reacting the corresponding benzoic acid derivatives, advantageously their lower alkyl esters or halides, with the respective nitrogen bases. The starting material mentioned under items (c) and (d) as well as the process intermediates thereof, e.g the 1-R -3-R -2- (methoxy-dihydroxyor hydroxy dimethoxy-benzoylimino)-l,3-diazacycloalkanes, are new and are considered as additional subject matter of the present invention. They also exhibit central nervous system depressing effects similar to those observed with the compounds of Formulae I or II. Preferred are the compounds mentioned under item (d) which yield the products of Formula II, i.e. those corresponding to Formulae HI and IV wherein each of p and q is an integer from 0 to 2 and p-l-q is not greater than 2, Z is either nitrogen or the moiety H-lilRs and R is 3,4,5-trimethoxybenzoyl, or acid addition salts thereof.

The pharmacologically active compounds of the invention are useful in the manufacture of pharmaceutical compositions containing an effective amount thereof in conjunction or admixture with excipients suitable for either enteral or parenteral application. Preferred are tablets and gelatin capsules comprising the active ingredient together with (a) diluents, e.g. lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and/or glycine, (b) lubricants, e.g. silica, talcum, stearic acid, its magnesium or calcium salt and/or polyethyleneglycol, for tablets also (0) binders, e.g. magnesium aluminum silicate, starch paste, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose and/or polyvinylpyrrolidone, if desired, (d) disintegrats, e.g. starches, agar, alginic acid or its sodium salt, enzymes of the binders or effervescent mixtures and/or (e) adsorbents, colorants, flavors and sweeteners. Injectable compositions are preferably aqueous isotonic solutions or suspensions, and suppositories are advantageously fatty emulsions or suspensions. They may be sterilized and/or contain adjuvants, such as preserving, stabilizing, wetting or emulsifying agents, solution promoters, salts for regulating the osmotic pressure and/or buffers. They may also contain other therapeutically valuable substances. Said pharmaceutical compositions are prepared according to conventional mixing, granulating or coating methods respectively and contain about 0.1 to 75%, preferably about 1 to 50% of the active ingredient.

The following examples are intended to illustrate the invention and are not to be construed as being limitations thereon. Temperatures are given in degrees centigrade, and all parts wherever given are parts by weight.

Example 1 To the solution obtained from- 5.76 g. sodium and ml. anhydrous methanol, 48.58 g. l-methyl-Z-imino-hexahydropyrimidine hydrobromide are added while stirring and cooling. After /2 hour, the mixture is evaporated in vacuo on the water bath for 4 hours. Hereupon ml. tetrahydrofuran are added under nitrogen followed by the solution of 28.8 g. 3,4,5-trimethoxybenzoyl chloride in ml. tetrahydrofuran during 35 minutes at 5-10 While stirring. After stirring overnight a room temperature, the mixture is poured onto 770 ml. ice and water and 21.2 g. sodium bicarbonate are added while stirring. The mixture is extracted three times with 100 ml. methylene chloride, the extract dried, filtered and evaporated below 40. Then residue is triturated with 45 ml. diethyl ether for 1 hour at room temperature, the mixture filtered and the residue washed with cold diethyl ether, to yield the 1 methyl-2-(3,4,S-trimethoxybenzoylimino)-hexahydropyrimidine of the formula it =N-C omelting at 142-145.

O CH:

The starting material is prepared as follows. To the mixture of 97.6 g. 3-methylamino-propylamine and 270 ml. methanol, the solution of 118 g. cyanogen bromide in 270 ml. methanol is added dropwise during 2 hours at -15 while stirring. After stirring at room temperature overnight, the mixture is refluxed for 6 hours and evaporated in vacuo. The residue is recrystallized from 217 ml. hot isopropanol and dried for 5 hours in vacuo, to yield the 1-methyl-2-imino-hexahydropyrimidine hydrobromide melting at 142-144".

Example 2 To the solution obtained from 2.3 g. sodium and 40 ml. methanol, 19.4 g. 1-methyl-2-imino-hexahydropyrimidine hydrobromide are added portionwise while stirring. After the initial lumps formed are dissolved, the mixture is evaporated in vacuo at room temperature for about 3 hours. The dry residue is slurried in 40 ml. tetrahydrofuran and 30 ml. triethylamine, whereupon the solution of 23 g. 3,4,5-trimethoxybenzoyl chloride in 50 ml. tetrahydrofuran is added during 15 minutes at 5-15" while stirring. The mixture is stirred at room temperature overnight and evaporated in vacuo. The residue is shaken with 60 ml. methylene chloride and 60 ml. aqueous ammonia, and the aqueous phase Washed with methylene chloride. The combined organic solution is washed with 30 ml. water dried, filtered and evaporated in vacuo. The residue is taken up in 60 ml. benzene and the solution extracted with 30 ml. water and 30 ml. hydrochloric acid. The combined aqueous layer is made basic with ammonia, the precipitate formed filtered 01f, washed with water, dried recrystallized from tetrahydrofuran, to yield the 1- methyl 2 (3,4,5-trimethoxybenzoylimino)-3-(3,4,5-trimethoxybenzoyl)-hexahydropyrimidine of the formula CHaO OCH

melting at 206-208.

Example 3 Preparation of 1000 tablets each containing 250 mg. of the active ingredient:

Formula: G.

1 methyl-2-(3,4,S-trimethoxybenzoylimino)- hexahydropyrimidine 250.0 Wheat starch 346.8 Magnesium aluminum silicate 20.0 Methylcellulose 13.3 Stearic acid 13.3 Colloidal silica 6.6

Anhydrous ethanol, q.s. Purified water, q.s.

Procedure: All powders with the exception of the silica and 96.8 g. of the starch are passed through a screen having openings of 0.6 mm. and mixed well. From the remaining starch and 65 ml. water a paste is formed which is used to granulate the powders together with the ethanol. The wet granulate is passed through a screen with 2 mm. openings and dried overnight at 35. The dry granulate is broken in a hammer mill, passed through a screen with 1.2 mm. openings and compressed into tablets each weighing 0.65 g., using concave punches with 12 mm. diam eter, uppers quartered.

Example 4 To the solution of 1 g. 1-methyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine in 5 ml. pyridine, 1 ml. acetic anhydride is added and the mixture allowed to stand at room temperature for 2 days. It is evaporated in, vacuo, the residue dissolved in 2 ml. hot tetrahydrofuran and the precipitate formed after cooling filtered 01?, to

8 yield the 1 methyl-3-acetyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine of the formula H 0 on,

To the solution of 5 g. 2 (3,4,5-trimethoxybenzoy1- imino)-hexahydropyrimidine in 50 ml. dimethylformamide, 0.7 g. of 57% sodium hydride in mineral oil are added and the mixture stirred for 1 hour at room temperature. After cooling to 5, the mixture of 1.5 ml. ethyl iodide and 12 ml. dimethylformamide is added dropwise during 7 minutes and the mixture stirred 3 hours at room temperature. It is diluted with 180 ml. ice water, extracted with methylene chloride, the extract dried, filtered and evaporated. The residue is triturated with 15 ml. cyclohexane, filtered off and washed with cyclohexane, to yield the 1 ethyl-2-(3,4,S-trimethoxybenzoylimino)-hexahydropyrimidine of the formula 'methoxybenzoylimino)-hexahydropyrimidine is prepared,

melting at 106-107.

The starting material is prepared as follows: To the solution obtained from 2.3 g. sodium and 50 ml. methanol, 18 g. 2-imino-hexahydropyrimidine hydrobromide are added while stirring and cooling. After /2 hour, 22.6 g. methyl 3,4,5-trimethoxybenzoate are added, the mixture stirred /2 hour at room temperature and gradually heated to the internal temperature of about 150 while distilling off methanol. Said temperature is maintained for /2 hour and the mixture evaporated in the vacuuo of a water-jet pump. The residue is taken up in 20 ml. water, the mixture ex tracted with 60 ml. methylene chloride, the extract dried, filtered and evaporated. The residue is taken up in 30 ml. hot benzene, the solution cooled, the crystals formed filtered off, dissolved in 80 ml. methanol, the solution concentrated to half the volume, the precipitate formed filtered off and washed with methanol, to yield the 2-(3,4, S-trimethoxybenzoylimino)-hexahydropyrimidine melting at 18l-183. From the combined mother liquors another crop thereof can be obtained.

By replacing the 18 g. Z-imino-hexahydropyrimidine hydrobromide by 19.4 g. of its l-rnethyl derivative, and following the procedure given, the compound of Example 1 is obtained.

Example 6 To the solution of 5 g. 2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine in 50 ml. dimethylformamide, 0.7 g. of 57% sodium hydride in mineral oil are added and the mixture stirred for 1 hour at room temperature. After cooling to 5, the mixture of 1.5 ml. allyl chloride and 11.5 ml. dimethylformamide is added dropwise during 7 minutes and the mixture stirred 3 hours at room temperature. It is diluted with ml. ice water, extracted with methylene chloride, the extract dried, filtered and evaporated. The residue is triturated with 15 ml. pentane, taken up in the minimum amount of benzene and the solution chromatographed on 75 g. aluminum oxide. 200 ml. of the first benzene eluate are collected, evaporated and the residue recrystallized from methanol,

to yield the 1-allyl-2-(3,4,5-trimethoxybenzoylimino)- hexahydrpyrirnidine of the formula oHz-GH=OH,

I CHa -N CO OCHa N CH:

melting at 144-146".

Example 7 melting at 201-203.

The starting material is prepared as follows: To the mixture of 60.1 g. ethylene diamine and 100 ml. methanol, the solution of 106 g. cyanogen bromide in 100 ml. methanol is added dropwise during 90 minutes while stirring and keeping the temperature below 10. The mixture is stirred at room temperature overnight, refluxed for 6 hours and evaporated in vacuo. The residue is recrystallized several times from isopropanol, to yield the 2- imino-imidazolidine hydrobromide melting at 125-129".

16.6 g. thereof are added to the solution obtained from 2.3 g. sodium and 40 ml. methanol, and the mixture is stirred for /2 hour at room temperature. Hereupon 22.6 g. methyl 3,4,5-trimethoxy-benzoate are added and the mixture stirred for /2 hour at room temperature. It is slowly concentrated, the concentrate stirred at 140-150 for /2 hour and finally evaporated at 12 mm. Hg. The residue is taken up in 60 ml. water, the mixture extracted with methylene chloride, the extract filtered and evaporated. The residue is triturated with 40 ml. diethyl ether and recrystallized from methanol, to yield the 2-(3,4,5-tri methoxybenzoylimino)-imidazolidine melting at 149- 150.

Example 8 To the solution of 1 g. 1-methyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine in 20 ml. dimethylformamide, 0.137 g. 56.8% sodium hydride in mineral oil are added and the mixture stirred at room temperature for '1 hour. It is cooled to about 0.21 ml. methyl iodide in 2 ml. dimethylformamide are added dropwise at said temperature and the mixture is stirred for 3 hours at room temperature. It is diluted with 60 ml. water and ml. saturated aqueous sodium chloride, extracted with methylene chloride, the extract dried, filtered and evaporated. The residue is recrystallized from tetrahydrofuran, to yield the 1,3-dimethyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine of the formula melting at 184-186.

Example 9 To the solution of 0.586 g. 2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine in 5.8 ml. dimethylformamide, 0.288 g. Z-dimethylaminoethyl chloride hydrochloride and 0.256 g. potassium hydroxide are added and the mixture stirred at room temperature for 22 hours. It is diluted with 24 ml. ice water, extracted with methylene chloride, the extract dried and evaporated. The residue is taken up in diethyl ether, the solution filtered and the filtrate concentrated, to yield the I-(Z-dimethylaminoethyl) 2 (3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine of the formula cm-cm-mcrm,

ci Fl melting at 88-90".

O CH:

Example 10 C m-CHT-Nwm ---N -C O 0 CH: -N

melting at 129-131.

Example 11 To the solution of 2.65 g. 1-methyl-2-galloyliminohexahydropyramidine in 30 ml. methanol, 33 ml. N- ethereal diazomethane are added dropwise while stirring and the mixture is allowed to stand overnight at room temperature. Hereupon a few drops acetic acid are added, the mixture evaporated in vacuo and the residue taken up in 5% aqueous sodium carbonate. The mixture is extracted with methylene chloride, the extract dried, filtered, evaporated and the residue is triturated with diethyl ether, to yield the 1-methyl-2-(3,4,5 trimethoxybenzoylimino)-hexahydropyrimidine, melting at 142- 145; it is identical with the compound obtained according to Example 1.

The starting material is prepared as follows: The mixture of 9.2 g. methyl gallate, 20 ml. methanol and 5.7 g. 1-methyl-2-imino-hexahydropyrimidine is slowly concentrated to reach a temperature between -150. After /2 hour the mixture is evaporated in vacuo, to yield the 1 methyl 2 galloylimino-hexahydropyrimidine, which is used as such without further purification.

Example 12 0.3 g. 1-methyl-2-(3,4,5 trimethoxybenzoylimino)-1, 2,3,4 tetrahydropyrimidine is hydrogenated in 10 ml. ethanol over 0.03 g. platinum catalyst at room temperature and atmospheric pressure. After the consumption of the theoretical amount of hydrogen, the mixture is filtered, the filtrate evaporated and the residue recrystallized from isopropanol, to yield the 1-methyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydr0pyrimidine, melting at 143-145"; it is identical with the compound obtained according to Example 1.

The starting material is prepared as follows: To the solution of 4.71 g. l-methyl-Z-imino-1,2-dihydropyrimidine hydroiodide in 47.4 ml. dimethylformamide, 0.845 g. 57% sodium hydride in mineral oil are added at 15 while stirring. After 1 hour the mixture is cooled to 5 and the solution of 2.3 g. 3,4,5-trimethoxybenzoyl chlo ride in 6.9 ml. tetrahydrofuran is added dropwise. After 3 hours stirring at room temperature, 160 ml. ice water and 0.7 g. potassium carbonate are added, the mixture extracted with methylene chloride, the extract dried, filtered and evaporated. The residue is triturated With ml. diethyl ether, filtered off and washed with diethyl ether. The residue is taken up in methylene chloride, the solution extracted with 10 ml. hydrochloric acid, the aqueous layer made basic with ammonia and extracted with methylene chloride. The extract is dried, evaporatd and the residue recrystallized from tetradrofuran, to yield the 1-methyl-2-(3,4,5-trimethoxybenzylimino)-1,2-dihydropyrimidine of the formula melting at 183-184.

To the solution of 0.4 g. thereof in 8 ml. methanol, 0.4 g. sodium borohydride are added portionwise while stirring and the mixture is allowed to stand at room temperature for 1 hour. It is diluted with 16 ml. ice water, the precipitate formed filtered off, washed with water and recrystallized from methanol, to yield the 1-methyl-2-(3, 4,5 trimethoxybenzoylimino)-1,2,3,4-tetrahydropyrimidine of the formula melting at 139141.

Example 13 Preparation of 10,000 capsules, each containing 250 mg. of the active ingredient: Formula: G.

1 allyl-2-(3,4,5 trimethoxybenzoylimino)- hexahydropyrimidine 2,500 Lactose 1,500 Talcum powder 300 Procedure: All the powders are passed through a screen with an opening of 0.6 mm. Then the drug susbtance is placed in a suitable mixer and mixed first with the talcum, then with the lactose until homogenous. No. 1 capsules are filled with 430 mg., using a capsule filling machine.

According to the above procedure or that of Example 3, capsules or tablets can be prepared containing any of the other active ingredients illustrated by the remaining examples.

Example 14 To the solution obtained from 1.15 g. sodium and ml. methanol, 9.7 g. 1-methyl-2-imino-hexahydropyrimidine hydrobromide are added while cooling and stirring. After /2 hour, 11.3 g. methyl, 2,4,5-trimethoxybenzoate are added and the whole stirred for /2 hour at room temperature. Hereupon the mixture is concentrated until the temperature reaches 140 and the mixture stirred for /2 hour at this temperature. It is evaporated in vacuo, the residue taken up in 20 ml. water, the solution extracted with methylene chloride, the extract dried, filtered and evaporated. The residue is taken up in 55 ml. hot benzene, the solution filtered and the precipitate formed after cooling filtered oil and washed with cold benzene. It is 12 triturated with 11.3 ml. cold methanol, filtered and the precipitate Washed with cold methanol, to yield the 1- methyl 2 (2,4,S-trimethoxybenzoylimino)-hexahydropyrimidine of the formula melting at l62164.

Example 15 To the solution of 4 g. 2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine in 40 m1. dimethylformamide, 0.63 g. 56.8% sodium hydride in mineral oil are added while stirring at 15 After stirring for /2 hour at room temperature, 1.4 ml. cyclopropylmethyl bromide are added and the whole stirred for /2 hour at room temcontinued for 18 hours at room temperature. The mixture is diluted with 120 ml. ice water, the precipitate formed filtered off and washed with water. It is dissolved in methylene chloride, the solution dried, filtered and evaporated. The residue is taken up in 4 ml. hot isopropanol and the precipitate formed after cooling filtered off and washed with cold isopropanol and pentane, to yield the 1 cyclopropylmethyl-2-(3,4,5-trimethoxybenzoylimino)- hexahydropyrimidine of the formula Q-oom melting at 120121.

By replacing the cyclopropylmethyl bromide by 1.84 ml. n-pentyl bromide and by following the procedure shown above, the 1-n-pentyl-2-(3,4,5-trimethoxybenzoylimino)-hexahydropyrimidine is obtained, melting at 110- 112.

OCH;

OCH;

Example 16 To the solution of 2.93 g. 1-methyl-2-syringoyliminiohexahydropyrimidine in 50 ml. methanol, 12 ml. N- ethereal diazomethane are added dropwise while stirring and the mixture allowed to stand overnight at room temperature. Hereupon one drop acetic acid is added, the mixture evaporated in vacuo and the residue taken up in 5% aqueous sodium carbonate. It is extracted with methylene chloride, the extract dried, evaporated and the residue recrystalliszed from isopropanol, to yield the 1- methyl 2 (3,4,5 trimethoxybenzoylimino)-hexahydropyrimidine, melting at 142145; it is identical With that obtained according to Examples 1, 11 and 12.

The starting material is prepared as follows: To the mixture of 15.1 g. methyl 4-benzyloxy- 3,5 dimethoxybenzoate and ml. toluene, 5.6 g. 1-methyl-2-imino hexahydropyrimidine are added, the mixture refluxed for 1 day under nitrogen and evaporated in vacuo. The residue is taken up in 143 ml. methanol, the solution concentrated and the precipitate formed filtered 01f, to yield the 1-methyl-2-(4 benzyloxy 3,5- dimethoxybenzoylimino)-hexahydropyrimidine melting at 147-149". The solution of 19.1 g. thereof in ml. toluene and 50 ml. methanol is hydrogenated over 1.91 g. 10% palladium on charcoal until 1.12 liter hydrogen have been absorbed. The mixture is combined With 150 ml. methylene chloride-methanol (2:1), filtered, the filtrate evaporated in vacuo and the residue recrystallized from methylene chloride-isopropanol, to yield the 1-methyl-2-syringoyli-minohexahydropyrimidine, melting at 229-231".

Example 17 To the solution of 2 g. of 2-(3,4,5-trimethoxybenzoyl- 1m1no)imidazolidine in 20 ml. of dimethylformamide, 0.3

melting at 152153.

Example 18 Preparation of 1,000 capsules, each containing 50 mg. of the active ingredient:

Formula: G.

1-methyl-2-(3,4,5 trimethoxybenzoylimino)- hexahydropyrimidine 50.0 Lactose 200.0 Talcum powder 30.0 Sodium lauryl sulfate 8.0 Magnesium stearate 12.0

Procedure: All the powders are passed through a screen with 0.6 mm. openings and mixed in a suitable mixer until homogenous. No. 1 capsules are filled with 400 mg., using a capsule filling machine.

Example 19 To the solution of 1.53 g. of 2-(3,4,5-trimethoxybenzoylimino) hexahydro 1,3 diazepine in 15 ml. of dimethylformamide, 0.232 g. of 57%- sodium hydride in mineral oil are added while stirring at room temperature. After 3 hours, an almost clear solution is obtained, which is cooled to 5, and the mixture of 0.34 ml. of methyl iodide and 3.4 ml. of dimethylformamide is added drop wise at this temperature. After stirring for 18 hours at room temperature, the mixture is diluted with 60 ml. of ice Water, the precipitate formed filtered otf after 15 minutes, washed with water and pentane and recrystallized from ethanol, to yield the 1-methyl 2 (3,4,5 trimethoxybenzoylimino)-hexahydro-1,3 diazepine of the formula melting at 141142.

The starting material is prepared as follows: To the mixture of 88.15 g. of 1,4-diaminobutane and 200 ml. of water, 196 ml. of concentrated hydrochloric acid are added dropwise while stirring. The resulting solution is cooled to room temperature and added durin 3 minutes to the mixture of 104 .g. nitroguanidine, 126.5 g. of potassium hydroxide and 500 ml. of water. The suspension obtained is stirred for 30 minutes at 65-70", slowly cooled to 2, filtered and the precipitate washed with 500 m1. of ice water. It is taken up in 510 ml. of 15% hydrochloric acid, the mixture filtered through diatomaceous earth, the residue washed with 500 ml. of water, the filtrate cooled to 0 and the precipitate formed filtered off to yield the 2-nitroimino-hexahydro 1,3 diazepine, melting at 225- 227.

The mixture of g. thereof, 100 ml. of aqueous acetic acid and 1 g. of 10% palladium on charcoal is hydrogenated at room temperature and atmospheric pressure until 2.88 It. of hydrogen have been absorbed. It is filtered, the residue washed with methanol, the filtrate combined with 8.36 ml. of concentrated hydrochloric acid and evaporated under reduced pressure. The residue is taken up in methylene chloride, the solution dried, filtered, evaporated and the residue dried at very low pressure and room temperature, to yield the 2-imino-hexahydro-1,3-diazepine hydrochloride, melting at 1l61l8.

9 g. thereof are added to the solution of 3.26 g. of sodium methylate in 20 ml. of methanol and the mixture stirred for 30 minutes at room temperature. Hereupon 13.6 g. of methyl 3,4,5-trimethoxybenzoate are added, the mixture stirred for /2 hour at room temperature, slowly concentrated and the concentrate stirred for another /2 hour at 140-150. It is finally evaporated at 12 mm. Hg, the residue taken up in water, the mixture extracted with methylene chloride, the extract dried and evaporated. The residue is swirled with 64 ml. of diethyl ether, the precipitate filtered off, dissolved in methylene chloride and chromatographed on 128 g. of magnesia-silicagel and the column eluted with 1.5 It. of methylene chloride. The eluate is evaporated and the residue recrystallized from methylene chloride-diethyl ether (1:10), to yield the 2- (3,4,5-trimethoxybenzoylimino)-hexahydro 1,3 diazepine, melting at 134-136.

Example 20 To the solution of 2.93 g. of 2-(3,4,5-trimethoxybenzoylimino)-imidazolidine in 30 ml. of dimethylformamide, 0.464 g. of 57% sodium hydride in mineral oil are added and the mixture stirred for 1 hour. It is cooled to 5, and 1.25 ml. of cyclopentyl bromide are added dropwise during 5 minutes. Thereupon the mixture is stirred at room temperature overnight, diluted with ml. of ice water and extracted with methylene chloride. The extract is dried, evaporated and the residue crystallized from methanol, to yield the l-cyclopentyl-Z-(3,4,5-trimethoxybenzoylimino)-imidazolidine of the formula "-I OCH: N NH 00113 N-CO OCH:

showing in the LR. spectrum bands at 1120, 1580 and 3180 cmr What is claimed is:

1. A 5 to 7 ring-membered 1-R -2-trimethoxybenz0ylimino-1,3-diazacycloalkane of the formula C I'LR,

in which R is alkyl, alkenyl or alkynyl, each with up to 4 carbon atoms, (hydroxy, alkoxy or dialkylamino)- alkyl wherein alkyl contains up to 4 carbon atoms and the oxygen or nitrogen atom is separated from the ringnitrogen atom by at least 2 carbon atoms, 3 to 7 ringmembered unsubstituted cycloalkyl, cycloalkenyl, (cyclw alkyl or cycloalkenyl) C-l to 4 alkyl, R is trimethoxybenzoyl, R is hydrogen alkyl or alkanoyl each with up to 4 carbon atoms and alk is alkylene containing and separating the adjacent nitrogen atoms by 2 to 4 carbon atoms, or a therapeutically acceptable acid addition salt thereof.

2. A compound as claimed in claim 1, in which formula R is alkyl, alkenyl or alkynyl with up to 4 carbon atoms, or (hydroxy, alkoxy or dialkylamino)-alkyl wherein alkyl contains up to 4 carbon atoms and the oxygen or nitrogen atom therein is separated from the ring-nitrogen atom by at least 2 carbon atoms, R is 2,3,4-, 2,4,5- or 3,4,5 trimethoxybenzoyl, R is hydrogen, alkyl or alkanoyl with up to 4 carbon atoms and alk is 1,2-ethylene, 1,2- or 1,3-propylene, 1,2-, 1,3-, 1,4- or 2,3-butylene, or a therapeutically acceptable acid addition salt thereof.

16 3. A compound as claimed in claim 1 and having the 5. A compound as claimed in claim 3 and being the formula 1-methyl-2-(3,4,S-trimethoxybenzoylimino) hexahydro- OCHa pyrimidine or a therapeutically acceptable acid addition N-R4 salt thereof. (0H,) C=NCO OCH; 5 References Cited Z UNITED STATES PATENTS 3,627,889 12/1971 Lucas et a1 260256 .4 H 1n WhlCh R is methyl, ethyl, n-propyl, allyl or Z-dunethyl- 3,655,895 4/1972 Lucas et a1 4 H aminoethyl, R is hydrogen, methyl or acetyl and n is an integer from 2 to 4, or a therapeutically acceptable 10 RICHARD J GALLAGHER, P i E i acid addition salt thereof.

4. A compound as claimed in claim 3, in Which for- US. Cl. X.R. l R4 is h ethyl 1134 l' 260-239 BC, 309.6, 304.7, 256.5 R; 424- 200, 232, 244, aminoethly, R 1s hydrogen, methyl or aceyl and 11 Is 251 273 the integer 3 or a therapeutically acceptable acid addition 15 salt thereof. 

